Sugar alcohols, a class of polyols, are commonly added to foods because of their lower caloric content than sugars; however, they are also, in general, less sweet, and are often combined with high-intensity sweeteners. They are also added to chewing gum because they are not broken down by bacteria in the mouth or metabolized to acids, and thus do not contribute to tooth decay. Maltitol, sorbitol, xylitol, erythritol, and isomalt are some of the more common types. Sugar alcohols may be formed under mild reducing conditions from their analogue sugars.
In polymer chemistry, polyols are compounds with multiple hydroxyl functional groups available for organic reactions. A molecule with two hydroxyl groups is a diol, one with three is a triol, one with four is a tetrol and so on.
Monomeric polyols such as glycerin, pentaerythritol, ethylene glycol and sucrose often serve as the starting point for polymeric polyols. These materials are often referred to as the "initiators" and reacted with propylene oxide or ethylene oxide to produce polymeric polyols. However, they should not be confused with free radical "initiators" used to promote other polymerization reactions. The functional group used as the starting point for a polymeric polyol need not be a hydroxyl group; there are a number of important polyols which are built up from amines. A primary amino group (-NH2) often functions as the starting point for two polymeric chains, especially in the case of polyether polyols.
Polymeric polyols are generally used to produce other polymers. They are reacted with isocyanates to make polyurethanes used to make mattresses, foam insulation for appliances (refrigerators and freezers), home and automotive seats, elastomeric shoe soles, fibers (e.g. Spandex), and adhesives.
Polymeric polyols are usually polyethers or polyesters. Polyether polyols are made by reacting epoxides like ethylene oxide or propylene oxide with the multifunctional initiator in the presence of a catalyst, often a strong base such as potassium hydroxide or a double metal cyanide catalyst such as zinc hexacyanocobaltate-t-butanol complex. Common polyether diols are polyethylene glycol, polypropylene glycol, and poly(tetramethylene ether) glycol. The examples shown below are fairly low molecular weight triols based on glycerin (a triol) being reacted with propylene oxide, ethylene oxide or a combination of the two. In reality, the chains would not be of equal length in any one molecule and there would be a distribution of molecular weight polyols within the material. Polyether polyols account for about 90% of the polymeric polyols used industrially; the balance is polyester polyols.
Another class of polymeric polyols is the polyesters. Polyesters are formed by condensation or step-growth polymerization of diols and dicarboxylic acids (or their derivatives), for example diethylene glycol reacting with phthalic acid. Alternatively, the hydroxyl group and the carboxylic acid (or their derivatives) may be within the same molecule, as in the case of caprolactone. The example below is an idealized structure that could be obtained by reacting pentaerythritol (a tetrol) with gamma-butyrolactone.
- "Polyols information source". www.Polyol.org. Retrieved 2010-03-10.
- Chinn, Henry; Akihiro Kishi and Uwe Loechner (April 2006). "Polyether Polyols for Urethanes (abstract only without subscription)". SRI Consulting.
- Alper, H.; J. L. Garcia; E. J. Jang (4 September 2002). "New heterogeneous catalysis for the synthesis of poly(ether polyol)s" (abstract). Journal of Applied Polymer Science 86 (7): 1553–1557. doi:10.1002/app.10996. Retrieved 2008-08-09.
- "Dow Polyurethanes and Thermoset Systems, uses and innovations". Archived from the original on 2007-09-13. Retrieved 2007-09-14.
- Kaszynski, Poitr; Oleg Kadkin; Karol Osajda; Thomas A. Barber (2003). "Polyester Polyols: Synthesis and Characterization of Diethylene Glycol Terephthalate Oligomers" (PDF). Journal of Polymer Science: Part A: Polymer Chemistry 41 (8): 1114–1123. Bibcode:2003JPoSA..41.1114K. doi:10.1002/pola.10655. Retrieved 2008-08-09.